Search for a relationship between molecular anomalies of the mutant erythrocyte pyruvate kinase variants and their pathological expression
- 1 April 1981
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 57 (2) , 172-175
- https://doi.org/10.1007/bf00282016
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Hereditary erythrocyte pyruvate-kinase (PK) deficiency and chronic hemolytic anemia: Clinical, genetic and molecular studies in six new Spanish patientsHuman Genetics, 1980
- Recommended Methods for the Characterization of Red Cell Pyruvate Kinase Variants.British Journal of Haematology, 1979
- Significance of the electrophoretic modifications of defective pyruvate kinase variants. Study of six new observationsClinica Chimica Acta; International Journal of Clinical Chemistry, 1979
- Pyruvate kinase-catalyzed ATP-formation in human red blood cell membranesAnnals of Hematology, 1978
- A spanish family with erythrocyte pyruvate kinase deficiency: Contribution of various immunologic methods in the study of the mutant enzymeClinica Chimica Acta; International Journal of Clinical Chemistry, 1977
- Effects of Sulphydryl Compounds on Abnormal Red Cell Pyruvate KinaseBritish Journal of Haematology, 1976
- Metabolie Regulation in Enzyme-Deficient Red CellsEnzyme, 1974
- Hemolytic Anemia and G6PD DeficiencyScience, 1973
- Clinical heterogeneity of erythrocyte pyruvate kinase deficiency. Evidence of an impaired utilization of ATP in a clinically severe form.1972
- An inherited molecular lesion of erythrocyte pyruvate kinaseJournal of Clinical Investigation, 1968